A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891582



Internal ID19185978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11606348..11787410hg38UCSC Ensembl
Outerchr9:11511860..11787410hg38UCSC Ensembl
Innerchr9:11606348..11787410hg19UCSC Ensembl
Outerchr9:11511860..11787410hg19UCSC Ensembl
Innerchr9:11596348..11777410hg18UCSC Ensembl
Outerchr9:11501860..11777410hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38275551
hg19275551
hg18275551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800417, essv25798790, essv25787190
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891582
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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